Office of Health Promotion and Disease Prevention, Department of Medicine, Emory University, Atlanta, GA 30303, USA.
Mayo Clin Proc. 2011 Aug;86(8):762-80. doi: 10.4065/mcp.2011.0128.
Statins (3-hydroxy-3-methylglutaryl-coenzyme A reductase inhibitors) represent the cornerstone of drug therapy to reduce low-density lipoprotein (LDL) cholesterol and cardiovascular risk. However, even optimal statin management of LDL cholesterol leaves many patients with residual cardiovascular risk, in part because statins are more effective in reducing LDL cholesterol than apolipoprotein B (Apo B). Apo B may be a better marker of atherogenic risk than LDL cholesterol because Apo B measures the total number of all atherogenic particles (total atherosclerotic burden), including LDL, very low-density lipoprotein, intermediate-density lipoprotein, remnant lipoproteins, and lipoprotein(a). To determine whether Apo B is a better indicator of baseline cardiovascular risk and residual risk after lipid therapy compared with LDL cholesterol, a MEDLINE search of the literature published in English from January 1, 1975, through December 1, 2010, was conducted. On the basis of data from most population studies, elevated Apo B was more strongly associated with incident coronary heart disease than similarly elevated LDL cholesterol. Apo B was also a superior benchmark (vs LDL cholesterol) of statins' cardioprotective efficacy in both primary-prevention and secondary-prevention trials. To minimize cardiovascular risk among persons with hypercholesterolemia or dyslipidemia, the best available evidence suggests that intensive therapy with statins should be initiated to achieve the lowest possible Apo B level (with adequate drug toleration) and then other therapies (eg, niacin, bile acid resins, ezetimibe) added to potentiate these Apo B-lowering effects. In future consensus lipid-lowering treatment guidelines, Apo B should be considered as an index of residual risk, a potential parameter of treatment efficacy, and a treatment target to minimize risk of coronary heart disease.
他汀类药物(3-羟基-3-甲基戊二酰辅酶 A 还原酶抑制剂)是降低低密度脂蛋白(LDL)胆固醇和心血管风险的药物治疗基石。然而,即使是最佳的他汀类药物 LDL 胆固醇管理,也会使许多患者存在残余的心血管风险,部分原因是他汀类药物在降低 LDL 胆固醇方面比载脂蛋白 B(Apo B)更有效。Apo B 可能是比 LDL 胆固醇更好的动脉粥样硬化风险标志物,因为 Apo B 测量所有致动脉粥样硬化颗粒(总动脉粥样硬化负担)的总数,包括 LDL、极低密度脂蛋白、中间密度脂蛋白、残粒脂蛋白和脂蛋白(a)。为了确定 Apo B 是否比 LDL 胆固醇更好地指示基线心血管风险和脂质治疗后的残余风险,对 1975 年 1 月 1 日至 2010 年 12 月 1 日期间发表的英文文献进行了 MEDLINE 搜索。基于大多数人群研究的数据,升高的 Apo B 与冠心病事件的相关性比类似升高的 LDL 胆固醇更强。Apo B 也是他汀类药物在一级预防和二级预防试验中心脏保护疗效的更好基准(vs LDL 胆固醇)。为了最大限度地降低患有高胆固醇血症或血脂异常的患者的心血管风险,最佳现有证据表明,应开始使用他汀类药物进行强化治疗,以达到尽可能低的 Apo B 水平(在可耐受药物的情况下),然后添加其他治疗方法(例如烟酸、胆汁酸树脂、依折麦布)以增强这些降低 Apo B 的作用。在未来的共识降脂治疗指南中,Apo B 应被视为残余风险的指标、治疗效果的潜在参数以及降低冠心病风险的治疗目标。